A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841142



Internal ID22616077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137116396..137125374hg38UCSC Ensembl
chr5:136452085..136461063hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg388979
hg198979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495536
Samples
Known GenesSPOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer